Product Details

SNP ID

rs113577701

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:84888838 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GATCAGGAGCAGCTGGAGCGAGGCG[A/G]CGCCGAAGCCCTTCTCCAGATGGTA

Phenotype

MIM: 606207

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

SLC28A1 PubMed Links

Gene Details

Gene

SLC28A1

Gene Name

solute carrier family 28 member 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001287761.1	369	Missense Mutation	ACG,GCG	T55A	NP_001274690.1
NM_001287762.1	369	Missense Mutation	ACG,GCG	T55A	NP_001274691.1
NM_001321721.1	369	Missense Mutation	ACG,GCG	T55A	NP_001308650.1
NM_001321722.1	369	Missense Mutation	ACG,GCG	T55A	NP_001308651.1
NM_004213.4	369	Missense Mutation	ACG,GCG	T55A	NP_004204.3
NM_201651.2	369	Missense Mutation	ACG,GCG	T55A	NP_964014.1
XM_011522203.2	369	Missense Mutation	ACG,GCG	T55A	XP_011520505.1
XM_011522204.2	369	Missense Mutation	ACG,GCG	T55A	XP_011520506.1
XM_011522205.2	369	Missense Mutation	ACG,GCG	T55A	XP_011520507.1
XM_011522206.2	369	Missense Mutation	ACG,GCG	T55A	XP_011520508.1
XM_011522207.2	369	Missense Mutation	ACG,GCG	T55A	XP_011520509.1
XM_011522208.2	369	Intron			XP_011520510.1
XM_011522209.2	369	Missense Mutation	ACG,GCG	T55A	XP_011520511.1
XM_011522210.2	369	Missense Mutation	ACG,GCG	T55A	XP_011520512.1
XM_011522211.2	369	Intron			XP_011520513.1
XM_011522212.1	369	Missense Mutation	ACG,GCG	T55A	XP_011520514.1
XM_011522214.2	369	Missense Mutation	ACG,GCG	T55A	XP_011520516.1
XM_011522215.2	369	Missense Mutation	ACG,GCG	T55A	XP_011520517.1
XM_011522216.2	369	Intron			XP_011520518.1
XM_011522217.1	369	Missense Mutation	ACG,GCG	T55A	XP_011520519.1
XM_011522218.2	369	Missense Mutation	ACG,GCG	T55A	XP_011520520.1
XM_017022723.1	369	Missense Mutation	ACG,GCG	T55A	XP_016878212.1

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